Canonical Allele Identifier: CA352204387

Gene: SLC25A38

Linked Data

• dbSNP Id: rs1468860486
• MyVariant Identifiers: chr3:g.39435903C>G (hg19) ; chr3:g.39394412C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394412C>G , CM000665.2:g.39394412C>G	GRCh38
NC_000003.11:g.39435903C>G , CM000665.1:g.39435903C>G	GRCh37
NC_000003.10:g.39410907C>G	NCBI36
NG_016931.1:g.16089C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.580C>G	ENSP00000495376.1:p.Gln194Glu
ENST00000643672.1:c.577C>G	ENSP00000494532.1:p.Gln193Glu
ENST00000645280.1:c.574C>G	ENSP00000496690.1:p.Gln192Glu
ENST00000645630.1:c.448C>G	ENSP00000493714.1:p.Gln150Glu
ENST00000648579.1:c.722-38C>G	ENSP00000497638.1:n.722-38C>G
ENST00000650617.1:c.628C>G MANE Select	ENSP00000497532.1:p.Gln210Glu
ENST00000273158.8:c.628C>G	ENSP00000273158.3:p.Gln210Glu
NM_017875.2:c.628C>G	NP_060345.2:p.Gln210Glu
XM_006713214.1:c.616C>G	XP_006713277.1:p.Gln206Glu
XM_011533869.1:c.610C>G	XP_011532171.1:p.Gln204Glu
XM_011533870.1:c.577C>G	XP_011532172.1:p.Gln193Glu
XM_011533871.1:c.448C>G	XP_011532173.1:p.Gln150Glu
NM_001354798.1:c.626-1986C>G	NP_001341727.1:n.626-1986C>G
NM_017875.4:c.628C>G MANE Select	NP_060345.2:p.Gln210Glu
XM_006713214.2:c.616C>G	XP_006713277.1:p.Gln206Glu
XM_011533869.2:c.610C>G	XP_011532171.1:p.Gln204Glu
XM_024453611.1:c.574C>G	XP_024309379.1:p.Gln192Glu
NM_001354798.2:c.626-1986C>G	NP_001341727.1:n.626-1986C>G